Tetrafluoroethylene → Ethanesulfonic acid, 1,1,2,2-tetrafluoro-, sodium salt (1:1)

HRID 2206965Notes

Reaction equation

HRID 2206965 reaction equation
[S:1]([O-:4])([O-:3])=[O:2].[Na+:5].[Na+].[F:7][C:8]([F:12])=[C:9]([F:11])[F:10]>O>[F:7][CH:8]([F:12])[C:9]([F:11])([F:10])[S:1]([O-:4])(=[O:3])=[O:2].[Na+:5]

Participants

4

Conditions

Temperature
120 °C

Procedure

The sodium sulphite (201 g) was dissolved in water (600 mL) and taken in a 1000 mL Hastelloy reactor. Tetrafluoroethylene (150 g) was added to the reactor at −130° C. The temperature of the reactor was increased to 120° C. and maintained at 120° C. for 12 hours. The reactor was cooled to 25° C. and unreacted tetrafluoroethylene was vented off. The water of the reaction was removed from reaction mixture by azeotropic distillation to obtain a reaction mass. The reaction mass was extracted with hot ethanol using soxhlet apparatus. The ethanolic solution was concentrated to obtain pure sodium tetrafluoroethane sulfonate (100 g).

Workup

  1. customtaken in a 1000 mL Hastelloy reactor
  2. temperaturemaintained at 120° C. for 12 hours
  3. temperatureThe reactor was cooled to 25° C.
  4. customThe water of the reaction was removed from reaction mixture by azeotropic distillation
  5. customto obtain a reaction mass
  6. extractionThe reaction mass was extracted with hot ethanol using soxhlet apparatus
  7. concentrationThe ethanolic solution was concentrated

Sources & evidence

ORD record
ord-429142376b494d088084b38f5ed80ddc
Source dataset
uspto-grants-2016_06
Patent number
US09376379B2

Reaction notes

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